02.10.23 -- Solve Clinical Trial Consulting & Regulatory Challenges With Key Partners

Discover how PhlexRIM’s preconfigured business process automation helped the company rapidly build streamlined regulatory workflows and lifecycles aligned with their internal processes – increasing the efficiency and consistency of regulatory operations.

One of Premier Consulting’s differentiating offerings is the portfolio analysis: a high-level, integrated evaluation of the scientific, medical, regulatory, and commercial viability of each product within a sponsor’s portfolio.

TransPerfect Life Sciences supports clinical supply teams with an end-to-end labeling process that ensures compliance and reduces timelines to speed up regulatory approvals.

Preparing regulatory marketing applications to their successful conclusions is our focus.

Explore what YPrime's eClinical consultants can provide for life science customers, from trusted advice to expert support.

Beyond meeting compliance standards, pharmaceutical companies must implement the quality systems necessary to handle data in the local language, ensure data privacy, and minimize risk.

For over 25 years, we have been designing and running a broad range of early phase studies required for NDA submissions. We are experts in the design and conduct of early clinical development plans and stand-alone studies.

The developer of an investigative medicinal product (IMP) for advanced, recurrent, non-resectable cervical cancer engaged Premier Research to assist with screening and enrollment in a Phase 2 study in Europe. Find out the results of this partnership.

Get a free preliminary evaluation of your protocol design from a leading CRO in Eastern Europe.

This webinar discusses the expansion of International Market for Ensartini and RNAi Therapeutics in Oncology, from Skin Cancers to Liver Cancers.